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February 26, 2026Scientific Reports3 citationsOpen Access

The potential cytotoxic effect of recent universal adhesives with modified monomeric compositions on human gingival epithelial cells

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OEOmar Abd El-MaksoudNSNessma SultanHIHoda Saleh Ismail

Key Points

  • The study evaluates the cytotoxicity of universal adhesives on human gingival epithelial cells.
  • Cytotoxicity assessed using MTT, SRB, and ROS analyses
  • Experiments compared three recent universal adhesives with a standard adhesive
  • Data analyzed via ANOVA and Tukey’s post hoc tests with P ≤ 0.05
  • Universal adhesives showed varied cytotoxic effects at different concentrations
  • At 50% and 100% concentrations, most adhesives reduced cell viability compared to control
  • One adhesive maintained higher viability, indicating potential for safer formulation

Abstract

Abstract This study aimed to assess the cytotoxicity of three recent universal adhesives (UAs) with modified monomeric compositions compared to a typical adhesive containing bisphenol A-glycidyl methacrylate (Bis-GMA) and hydroxyethyl methacrylate (HEMA) on human gingival epithelial cells. Disk-shaped specimens of Scotchbond Universal Plus (SBP), Zipbond Universal (ZBU), Clearfil TRI-S Bond Universal Quick (CSQ), and Tetric N-Bond Universal (TNB) were fabricated and then kept in Dulbecco’s Modified Eagle Medium (DMEM) for 24 h to prepare the extract medium. Cytotoxicity was evaluated with MTT, SRB, and ROS analyses. Data were analysed by ANOVA and Tukey’s post hoc multiple comparison tests ( P ≤ 0.05). At both tested concentrations (50% & 100%), MTT results showed that SBP, ZBU, and TNB significantly reduced cell viability compared with the control, in contrast to CSQ, which exhibited the highest viability. Regarding SRB results, SBP, ZBU, and CSQ maintained cell viabilities comparable to the control and significantly higher than TNB at both concentrations. ELISA results revealed statistically significant differences in ROS levels among all tested UAs compared to the control and to each other. The cytotoxicity of UAs is both composition and concentration-dependent, with modified formulations showing relatively safer profiles reflecting the potential effect of modifying the monomeric formulations in enhancing cytocompatibility.

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Cite This Study

El-Maksoud et al. (2026) studied this question.

synapsesocial.com/papers/699f95ba1bc9fecf3dab3e9dhttps://doi.org/10.1038/s41598-026-38054-0
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